The CD4-specific monoclonal antibody (mAb) CC26, when tested on a tota
l of 143 cattle, failed to react with T cells from 16% of animals and
gave reduced intensity staining in a further 35% of animals. The resul
ts of family studies with groups of half- and full-siblings indicated
that CC26 recognizes an allele of CD4 which is co-dominantly expressed
in heterozygous animals. This was confirmed by sequential immunopreci
pitation and by selecting transfectants expressing the CC26(+) and CC2
6(-) allelic forms of CD4 following transfection of genomic DNA. from
a heterozygous animal. Biochemical studies also revealed an allelic di
fference in the relative molecular weight (M(r)) of the CD4 molecule,
one allele giving 49000/52000 MW bands and the other 52000/57000 MW ba
nds in sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS
-PAGE). Treatment of CD4(+) cell lines with tunicamycin resulted in th
e appearance of a 47000 MW band for both allelic forms indicating that
the difference in M(r) is due to glycosylation. All of the CC26(+) al
leles examined were of the low molecular weight form (M(r)(low)) where
as both M(r)(low) and M(r)(low) alleles were represented in CC26(-) an
imals. Thus, on the basis of M(r) and reactivity with mAb CC26, three
allelic forms of bovine CD4 can be identified, namely CC26(+) M(r)(low
), CC26(-) M(r)(low) and CC26(-) M(r)(high); it is proposed that these
alleles are designated CD4.1, CD4.2 and CD4.3, respectively. The alle
lic difference detected by CC26 was present in both Bos taurus and B.
indicus cattle indicating that it had arisen prior to divergence of th
ese subspecies. The M(r)(high) allele (CD4.3) was detected only in B.
indicus animals.